Abnormality of iron homeostasis
Symptom Information:
Symptom ID: | HPO:0011031 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of ion homeostasis(HPO:0003111) Abnormality of cation homeostasis(HPO:0010929) Abnormality of transition element cation homeostasis(HPO:0011030) Abnormality of iron homeostasis(HPO:0011031) MedDRA: |
||||||||||
Database Frequency: | 16 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia intermedia | (Orphanet:231222) |
Beta-thalassemia major | (Orphanet:231214) |
GRACILE syndrome | (Orphanet:53693) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Hemoglobin E - beta-thalassemia | (Orphanet:231249) |
Neonatal hemochromatosis | (Orphanet:446) |
Neurodegeneration with brain iron accumulation | (Orphanet:385) |
Rare hereditary hemochromatosis | (Orphanet:220489) |
Syndromic diarrhea | (Orphanet:84064) |